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Precision Diagnosis and Treatment Research on Membranous Nephropathy and IgA Nephropathy Based on Epitranscriptomics, Structural Immunity, and Cellular Senescence Mechanisms

Precision Diagnosis and Treatment Research on Membranous Nephropathy and IgA Nephropathy Based on Epitranscriptomics, Structural Immunity, and Cellular Senescence Mechanisms

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121518
Enrollment
Unknown
Registered
2026-03-31
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

primary membranous nephropathy (MN) and IgA nephropathy (IgAN)

Interventions

membrane nephrapathy group:None

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age 18 years or older; 2. Patients diagnosed with primary membranous nephropathy according to the 2021 KDIGO Clinical Practice Guideline for the Management of Glomerular Diseases; 3. Serum anti-PLA2R antibody positive; 4. No previous treatment with rituximab or calcineurin inhibitors (such as cyclosporine, tacrolimus), and no prior use of novel drugs specifically for MN; 5. If previously treated with glucocorticoids or alkylating agents, discontinuation for at least 6 months is required.

Exclusion criteria

Exclusion criteria: 1. Secondary MN clearly caused by other etiologies such as lupus, hepatitis, malignancy, or drugs. 2. Previous treatment with rituximab or calcineurin inhibitors (e.g., cyclosporine, tacrolimus), or receipt of novel drugs for MN. 3. Severe renal impairment: estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73m² (calculated using the MDRD formula). 4. Uncontrolled hypertension. 5. Active infection (including hepatitis B, hepatitis C, HIV). 6. Presence of other severe or unstable illnesses. 7. Neutropenia (neutrophil count < 1.5 x 10³/µL). 8. Thrombocytopenia (platelet count < 100,000/µL). 9. Any hematologic disorder, or disease affecting the hematopoietic system. 10. Current or prior (within six months before enrollment) use of drugs affecting the immune or hematopoietic system. 11. Pregnancy or lactation. 12. Patients of childbearing potential unwilling to use effective contraception during the study period. 13. Other populations deemed ineligible by the investigator or ethics committee.

Design outcomes

Primary

MeasureTime frame
Gene;

Countries

China

Contacts

Public ContactZibo Xiong

Peking University Shenzhen Hospital

xiong0301@163.com+86 177 0275 4846

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026